1wqj

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== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[1wqj]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1WQJ OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1WQJ FirstGlance]. <br>
<table><tr><td colspan='2'>[[1wqj]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1WQJ OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1WQJ FirstGlance]. <br>
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</td></tr><tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1h59|1h59]]</td></tr>
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</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1h59|1h59]]</td></tr>
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<tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1wqj FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1wqj OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1wqj RCSB], [http://www.ebi.ac.uk/pdbsum/1wqj PDBsum]</span></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1wqj FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1wqj OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1wqj RCSB], [http://www.ebi.ac.uk/pdbsum/1wqj PDBsum]</span></td></tr>
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<table>
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</table>
== Disease ==
== Disease ==
[[http://www.uniprot.org/uniprot/IGF1B_HUMAN IGF1B_HUMAN]] Defects in IGF1 are the cause of insulin-like growth factor I deficiency (IGF1 deficiency) [MIM:[http://omim.org/entry/608747 608747]]. IGF1 deficiency is an autosomal recessive disorder characterized by growth retardation, sensorineural deafness and mental retardation.
[[http://www.uniprot.org/uniprot/IGF1B_HUMAN IGF1B_HUMAN]] Defects in IGF1 are the cause of insulin-like growth factor I deficiency (IGF1 deficiency) [MIM:[http://omim.org/entry/608747 608747]]. IGF1 deficiency is an autosomal recessive disorder characterized by growth retardation, sensorineural deafness and mental retardation.
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</StructureSection>
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Engh, R A.]]
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[[Category: Engh, R A]]
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[[Category: Holak, T A.]]
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[[Category: Holak, T A]]
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[[Category: Huber, R.]]
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[[Category: Huber, R]]
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[[Category: Kuenkele, K P.]]
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[[Category: Kuenkele, K P]]
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[[Category: Lang, K.]]
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[[Category: Lang, K]]
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[[Category: Popowicz, G M.]]
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[[Category: Popowicz, G M]]
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[[Category: Siwanowicz, I.]]
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[[Category: Siwanowicz, I]]
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[[Category: Wisniewska, M.]]
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[[Category: Wisniewska, M]]
[[Category: Disulfide bond ladder]]
[[Category: Disulfide bond ladder]]
[[Category: Disulfide rich]]
[[Category: Disulfide rich]]
[[Category: Protein binding-hormone-growth factor complex]]
[[Category: Protein binding-hormone-growth factor complex]]
[[Category: Protein-protein complex]]
[[Category: Protein-protein complex]]

Revision as of 13:32, 6 January 2015

Structural Basis for the Regulation of Insulin-Like Growth Factors (IGFs) by IGF Binding Proteins (IGFBPs)

1wqj, resolution 1.60Å

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